Price D L, Sisodia S S
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2196, USA.
Annu Rev Neurosci. 1998;21:479-505. doi: 10.1146/annurev.neuro.21.1.479.
The most common cause of dementia occurring in mid- to late-life is Alzheimer's disease (AD). Some cases of AD, particularly those of early onset, are familial and inherited as autosomal dominant disorders linked to the presence of mutant genes that encode the amyloid precursor protein (APP) or the presenilins (PS1 or PS2). These mutant gene products cause dysfunction/death of vulnerable populations of nerve cells important in memory, higher cognitive processes, and behavior. AD affects 7-10% of individuals > 65 years of age and perhaps 40% of individuals > 80 years of age. For the late-onset cases, the principal risk factors are age and apolipoprotein (apoE) allele type, with apoE4 allele being a susceptibility factor. In this review, we briefly discuss the clinical syndrome of AD and the neurobiology/neuropathology of the disease and then focus attention on mutant genes linked to autosomal dominant familial AD (FAD), the biology of the proteins encoded by these genes, and the recent exciting progress in investigations of genetically engineered animal models that express these mutant genes and develop some features of AD.
中年至老年期痴呆最常见的病因是阿尔茨海默病(AD)。部分AD病例,尤其是早发型病例,具有家族性,呈常染色体显性遗传疾病,与编码淀粉样前体蛋白(APP)或早老素(PS1或PS2)的突变基因有关。这些突变基因产物会导致对记忆、高级认知过程及行为至关重要的脆弱神经细胞群功能障碍/死亡。AD影响7% - 10%的65岁以上个体,可能影响40%的80岁以上个体。对于晚发型病例,主要风险因素是年龄和载脂蛋白(apoE)等位基因类型,其中apoE4等位基因是一个易感因素。在本综述中,我们简要讨论AD的临床综合征以及该疾病的神经生物学/神经病理学,然后重点关注与常染色体显性家族性AD(FAD)相关的突变基因、这些基因所编码蛋白质的生物学特性,以及在表达这些突变基因并出现AD某些特征的基因工程动物模型研究方面最近取得的令人兴奋的进展。